Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → (S)-1-Benzyl-3-mesyloxypyrrolidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (S)-(-)-1-Benzyl-3-pyrrolidinol | HCID 2733875 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | (S)-1-Benzyl-3-mesyloxypyrrolidine | HCID 10934081 | 98% |
반응 단계
(S)-1-Benzyl-3-hydroxypyrrolidine (1003.5 g, 5.66 mol) was dissolved in toluene (12 L) and the solution stirred and cooled to 0°-5° C. Triethylamine (680 g, 6.67 mol) was added followed by methanesulfonyl chloride (760 g, 6.63 mol) over a 4 hour period. A slurry formed after 30 minutes. The mixture was allowed to stir an additional 1.5 hours and 7% sodium bicarbonate (12 L) was added to the reaction mixture and the organic layer separated. The aqueous layer was extracted with toluene (4 L and 2 L) and the combined organic layers washed with saturated sodium bicarbonate (3×6 L), dried over MgSO4 and concentrated under reduced pressure to give (S)-1-benzyl-3-mesyloxypyrrolidine as a yellow oil (1.41 kg, 98%):
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05466828 |
| 출처 데이터셋 | uspto-grants-1995_11 |
| ORD ID | ord-598cb616651a47af9cf13705182b4fa2 |
| 출처 메모 | uspto-grants-1995_11 |